RESUMEN
Mast cells (MCs) can release a variety of biologically active mediators under different circumstances, such as fever or vaccination. Our aim was to evaluate the incidence and severity of MC activation symptoms induced by SARS-CoV-2 virus (COVID-19) infection and vaccination in a cohort of 92 pediatric patients with cutaneous mastocytosis. Our findings support previous evidence on the safety of COVID-19 infection and vaccination in patients with MC disorders.
Asunto(s)
Vacunas contra la COVID-19 , COVID-19 , Mastocitosis Cutánea , SARS-CoV-2 , Adolescente , Niño , Preescolar , Femenino , Humanos , Lactante , Masculino , COVID-19/prevención & control , Vacunas contra la COVID-19/efectos adversos , Estudios Transversales , Estudios Retrospectivos , VacunaciónAsunto(s)
Diterpenos/administración & dosificación , Tejido de Granulación/efectos de los fármacos , Enfermedades de la Piel/tratamiento farmacológico , Anciano de 80 o más Años , Carcinoma de Células Escamosas/cirugía , Tejido de Granulación/patología , Humanos , Masculino , Cuero Cabelludo/patología , Enfermedades de la Piel/patología , Neoplasias Cutáneas/cirugía , Resultado del TratamientoRESUMEN
Acral persistent papular mucinosis (APPM) is a rare subtype of localized lichen myxedematosus. It consists of small papules localized exclusively on the back of the hands, wrists and extensor aspects of distal forearms with no other clinical or laboratory manifestations. The lesions tend to persist and may increase slowly in number. Histologically, hematoxylin-eosin and Alcian blue staining demonstrate mucin accumulation in the upper reticular dermis with separation of collagen fibers as a result of hyaluronic acid deposition. Treatment is rarely necessary due to the absence of symptoms. We present a 27-year-old healthy woman with asymptomatic papules on her upper extremities, which adequately meet clinical and pathological criteria of acral papular mucinosis.
Asunto(s)
Escleromixedema/patología , Enfermedades de la Piel/patología , Piel/patología , Adulto , Biopsia , Femenino , Humanos , Mucinas/análisis , Enfermedades Raras , Extremidad SuperiorRESUMEN
Abstract Acral persistent papular mucinosis (APPM) is a rare subtype of localized lichen myxedematosus. It consists of small papules localized exclusively on the back of the hands, wrists and extensor aspects of distal forearms with no other clinical or laboratory manifestations. The lesions tend to persist and may increase slowly in number. Histologically, hematoxylin-eosin and Alcian blue staining demonstrate mucin accumulation in the upper reticular dermis with separation of collagen fibers as a result of hyaluronic acid deposition. Treatment is rarely necessary due to the absence of symptoms. We present a 27-year-old healthy woman with asymptomatic papules on her upper extremities, which adequately meet clinical and pathological criteria of acral papular mucinosis.
Asunto(s)
Humanos , Femenino , Adulto , Piel/patología , Enfermedades de la Piel/patología , Escleromixedema/patología , Biopsia , Extremidad Superior , Enfermedades Raras , Mucinas/análisisAsunto(s)
Pustulosis Exantematosa Generalizada Aguda/diagnóstico , Fiebre/etiología , Pustulosis Exantematosa Generalizada Aguda/complicaciones , Pustulosis Exantematosa Generalizada Aguda/tratamiento farmacológico , Azitromicina/administración & dosificación , Azitromicina/uso terapéutico , Diagnóstico Diferencial , Quimioterapia Combinada , Femenino , Humanos , Leucocitosis/etiología , Persona de Mediana Edad , Prednisona/administración & dosificación , Prednisona/uso terapéutico , Psoriasis/diagnósticoRESUMEN
La mononucleosis infecciosa debe sospecharse en pacientes que cursan un cuadro pseudogripal que evoluciona a una faringoamigdalitis inespecífica y aparición de lesiones cutáneas, que frecuentemente se confunde con una infección bacteriana. Su expresión en la piel da lugar a dos tipos de exantemas. El primero, de aparición temprana, polimorfo y que resuelve en pocos días y otro, llamado sinérgico, relacionado con la administración de antibióticos. Presentamos el caso de una paciente con mononucleosis infecciosa que desarrolló un exantema de tipo sinérgico.
Infectious mononucleosis should be suspected in patients who have flu-like symptoms which progress to nonspecific pharyngitis and skin lesions. It is usually confused with a bacterial infection. Expression in the skin gives rise to two types of exanthemas. The first one, early-onset, polymorphous and early-resolution. The other one, also called synergic, related to antibiotics. We report a case of a patient with an infectious mononucleosis and a synergic exanthema.